コード例 #1
0
def test_damage_hyphae_0(
    neutrophil_list: NeutrophilCellList, grid: RectangularGrid, fungus_list: FungusCellList, iron
):
    n_det = 0
    n_kill = 2
    t = 1
    health = 100

    point = Point(x=35, y=35, z=35)
    neutrophil_list.append(
        NeutrophilCellData.create_cell(
            point=point, status=NeutrophilCellData.Status.NONGRANULATING, granule_count=5
        )
    )

    # hyphae
    fungus_list.append(
        FungusCellData.create_cell(
            point=point, status=FungusCellData.Status.RESTING, form=FungusCellData.Form.HYPHAE
        )
    )

    neutrophil_list.damage_hyphae(n_det, n_kill, t, health, grid, fungus_list, iron)

    assert fungus_list[0]['health'] == 50
    assert neutrophil_list[0]['granule_count'] == 4
    assert neutrophil_list[0]['status'] == NeutrophilCellData.Status.GRANULATING

    vox = grid.get_voxel(neutrophil_list[0]['point'])
    assert iron[vox.z, vox.y, vox.x] == 0
コード例 #2
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def test_damage_hyphae_conidia(
    neutrophil_list: NeutrophilCellList, grid: RectangularGrid, fungus_list: FungusCellList, iron
):
    n_det = 1
    n_kill = 2
    t = 1
    health = 100

    point = Point(x=35, y=35, z=35)
    neutrophil_list.append(
        NeutrophilCellData.create_cell(
            point=point, status=NeutrophilCellData.Status.NONGRANULATING, granule_count=5
        )
    )

    # conidia
    fungus_list.append(
        FungusCellData.create_cell(point=point, status=FungusCellData.Status.RESTING)
    )

    neutrophil_list.damage_hyphae(n_det, n_kill, t, health, grid, fungus_list, iron)

    assert fungus_list[0]['health'] == 100
    assert neutrophil_list[0]['granule_count'] == 5
    assert neutrophil_list[0]['status'] == NeutrophilCellData.Status.NONGRANULATING
コード例 #3
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def test_internalize_conidia_0(macrophage_list: MacrophageCellList,
                               grid: RectangularGrid,
                               fungus_list: FungusCellList):
    m_det = 0

    point = Point(x=35, y=35, z=35)
    macrophage_list.append(MacrophageCellData.create_cell(point=point))
    fungus_list.append(
        FungusCellData.create_cell(point=point,
                                   status=FungusCellData.Status.RESTING))

    vox = grid.get_voxel(macrophage_list[0]['point'])

    assert len(fungus_list.get_cells_in_voxel(vox)) == 1

    f_index = fungus_list.get_cells_in_voxel(vox)  # 0
    assert f_index == 0

    fungus_list[f_index]['form'] = FungusCellData.Form.CONIDIA
    fungus_list[f_index]['status'] = FungusCellData.Status.RESTING

    macrophage_list.internalize_conidia(m_det, 50, 1, grid, fungus_list)

    assert grid.get_voxel(fungus_list[f_index]['point']) == vox
    assert fungus_list.cell_data['internalized'][f_index]
    assert macrophage_list.len_phagosome(0) == 1
コード例 #4
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    def move(self, rec_r, grid, cyto, tissue, fungus: FungusCellList):
        for cell_index in self.alive():
            cell = self[cell_index]
            cell_voxel = grid.get_voxel(cell['point'])

            valid_voxel_offsets = []
            above_threshold_voxel_offsets = []

            # iterate over nearby voxels, recording the cytokine levels
            for dx, dy, dz in itertools.product((-1, 0, 1), repeat=3):
                zi = cell_voxel.z + dz
                yj = cell_voxel.y + dy
                xk = cell_voxel.x + dx
                if grid.is_valid_voxel(Voxel(x=xk, y=yj, z=zi)):
                    if tissue[zi, yj, xk] != TissueTypes.AIR.value:
                        valid_voxel_offsets.append((dx, dy, dz))
                        if cyto[zi, yj, xk] >= rec_r:
                            above_threshold_voxel_offsets.append(
                                (cyto[zi, yj, xk], (dx, dy, dz)))

            # pick a target for the move
            if len(above_threshold_voxel_offsets) > 0:
                # shuffle + sort (with _only_ 0-key, not lexicographic as tuples) ensures
                # randomization when there are equal top cytokine levels
                # note that numpy's shuffle will complain about ragged arrays
                shuffle(above_threshold_voxel_offsets)
                above_threshold_voxel_offsets = sorted(
                    above_threshold_voxel_offsets,
                    key=lambda x: x[0],
                    reverse=True)
                _, target_voxel_offset = above_threshold_voxel_offsets[0]
            elif len(valid_voxel_offsets) > 0:
                target_voxel_offset = choice(valid_voxel_offsets)
            else:
                raise AssertionError(
                    'This cell has no valid voxel to move to, including the one that it is in!'
                )

            # Some nonsense here, b/c jump is happening at the voxel level, not the point level
            starting_cell_point = Point(x=cell['point'][2],
                                        y=cell['point'][1],
                                        z=cell['point'][0])
            starting_cell_voxel = grid.get_voxel(starting_cell_point)
            ending_cell_voxel = grid.get_voxel(
                Point(
                    x=grid.x[cell_voxel.x + target_voxel_offset[0]],
                    y=grid.y[cell_voxel.y + target_voxel_offset[1]],
                    z=grid.z[cell_voxel.z + target_voxel_offset[2]],
                ))
            ending_cell_point = (starting_cell_point +
                                 grid.get_voxel_center(ending_cell_voxel) -
                                 grid.get_voxel_center(starting_cell_voxel))

            cell['point'] = ending_cell_point
            self.update_voxel_index([cell_index])

            for i in range(0, self.len_phagosome(cell_index)):
                f_index = cell['phagosome'][i]
                fungus[f_index]['point'] = ending_cell_point
                fungus.update_voxel_index([f_index])
コード例 #5
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ファイル: test_fungus.py プロジェクト: knappa/nlisim
def test_iron_uptake(populated_fungus: FungusCellList, iron):
    iron_min = 5
    iron_max = 100
    iron_absorb = 0.5
    assert iron[5, 5, 5] == 10

    populated_fungus.iron_uptake(iron, iron_max, iron_min, iron_absorb)

    for cell in populated_fungus.cell_data:
        assert cell['iron'] == 5
コード例 #6
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ファイル: test_fungus.py プロジェクト: knappa/nlisim
def populated_fungus(fungus_list: FungusCellList):
    points = []
    for i in range(10, 60, 10):
        points.append(Point(x=i, y=i, z=i))

    for point in points:
        fungus_list.append(
            FungusCellData.create_cell(
                point=point,
                status=FungusCellData.Status.GROWABLE,
                form=FungusCellData.Form.HYPHAE,
                iron=0,
                mobile=False,
            ))
    yield fungus_list
コード例 #7
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def test_sporeless30(macrophage_list: MacrophageCellList,
                     grid: RectangularGrid, fungus_list: FungusCellList):
    # should release all conidia

    point = Point(x=35, y=35, z=35)
    for _ in range(0, 30):
        macrophage_list.append(MacrophageCellData.create_cell(point=point))

    fungus_list.append(
        FungusCellData.create_cell(point=point,
                                   status=FungusCellData.Status.RESTING,
                                   form=FungusCellData.Form.HYPHAE))

    macrophage_list.remove_if_sporeless(0.3)
    assert len(macrophage_list.alive()) < 30
コード例 #8
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ファイル: neutrophil.py プロジェクト: knappa/nlisim
    def damage_hyphae(self, n_det, n_kill, time, health, grid,
                      fungus: FungusCellList, iron):
        for i in self.alive(self.cell_data['granule_count'] > 0):
            cell = self[i]
            vox = grid.get_voxel(cell['point'])

            # Moore neighborhood, but order partially randomized. Closest to furthest order, but
            # the order of any set of points of equal distance is random
            neighborhood = list(
                itertools.product(tuple(range(-1 * n_det, n_det + 1)),
                                  repeat=3))
            shuffle(neighborhood)
            neighborhood = sorted(neighborhood,
                                  key=lambda v: v[0]**2 + v[1]**2 + v[2]**2)

            for dx, dy, dz in neighborhood:
                zi = vox.z + dz
                yj = vox.y + dy
                xk = vox.x + dx
                if grid.is_valid_voxel(Voxel(x=xk, y=yj, z=zi)):
                    index_arr = fungus.get_cells_in_voxel(
                        Voxel(x=xk, y=yj, z=zi))
                    if len(index_arr) > 0:
                        iron[zi, yj, xk] = 0
                    for index in index_arr:
                        if (fungus[index]['form'] == FungusCellData.Form.HYPHAE
                                and cell['granule_count'] > 0):
                            fungus[index]['health'] -= health * (time / n_kill)
                            cell['granule_count'] -= 1
                            cell[
                                'status'] = NeutrophilCellData.Status.GRANULATING
                        elif cell['granule_count'] == 0:
                            cell[
                                'status'] = NeutrophilCellData.Status.NONGRANULATING
                            break
コード例 #9
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ファイル: epithelium.py プロジェクト: knappa/nlisim
    def internalize_conidia(self, e_det, max_spores, p_in, grid,
                            spores: FungusCellList):
        for i in self.alive():
            cell = self[i]
            vox = grid.get_voxel(cell['point'])

            # Moore neighborhood, but order partially randomized. Closest to furthest order, but
            # the order of any set of points of equal distance is random
            neighborhood = list(
                itertools.product(tuple(range(-1 * e_det, e_det + 1)),
                                  repeat=3))
            shuffle(neighborhood)
            neighborhood = sorted(neighborhood,
                                  key=lambda v: v[0]**2 + v[1]**2 + v[2]**2)

            for dx, dy, dz in neighborhood:
                zi = vox.z + dz
                yj = vox.y + dy
                xk = vox.x + dx
                if grid.is_valid_voxel(Voxel(x=xk, y=yj, z=zi)):
                    index_arr = spores.get_cells_in_voxel(
                        Voxel(x=xk, y=yj, z=zi))
                    for index in index_arr:
                        if (spores[index]['form']
                                == FungusCellData.Form.CONIDIA
                                and not spores[index]['internalized']
                                and p_in > rg.random()):
                            spores[index]['internalized'] = True
                            if self.append_to_phagosome(i, index, max_spores):
                                spores[index]['mobile'] = False
                            else:
                                spores[index]['internalized'] = False
コード例 #10
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    def produce_cytokines(self, m_det, m_n, grid, fungus: FungusCellList,
                          cyto):
        for i in self.alive():
            vox = grid.get_voxel(self[i]['point'])

            hyphae_count = 0

            # Moore neighborhood
            neighborhood = tuple(
                itertools.product(tuple(range(-1 * m_det, m_det + 1)),
                                  repeat=3))

            for dx, dy, dz in neighborhood:
                zi = vox.z + dz
                yj = vox.y + dy
                xk = vox.x + dx
                if grid.is_valid_voxel(Voxel(x=xk, y=yj, z=zi)):
                    index_arr = fungus.get_cells_in_voxel(
                        Voxel(x=xk, y=yj, z=zi))
                    for index in index_arr:
                        if fungus[index]['form'] == FungusCellData.Form.HYPHAE:
                            hyphae_count += 1

            cyto[vox.z, vox.y,
                 vox.x] = cyto[vox.z, vox.y, vox.x] + m_n * hyphae_count
コード例 #11
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def test_sporeless1(macrophage_list: MacrophageCellList, grid: RectangularGrid,
                    fungus_list: FungusCellList):
    # should release all conidia

    point = Point(x=35, y=35, z=35)
    macrophage_list.append(MacrophageCellData.create_cell(point=point))
    fungus_list.append(
        FungusCellData.create_cell(point=point,
                                   status=FungusCellData.Status.RESTING))

    if len(
            fungus_list.alive(fungus_list.cell_data['form'] ==
                              FungusCellData.Form.CONIDIA)) == 0:
        macrophage_list.remove_if_sporeless(0.1)
    assert not macrophage_list.cell_data[0]['dead']

    macrophage_list.remove_if_sporeless(0.1)
    assert macrophage_list.cell_data[0]['dead']
コード例 #12
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def test_kill_macrophage(macrophage_list: MacrophageCellList,
                         grid: RectangularGrid, fungus_list: FungusCellList):
    # should release all conidia

    point = Point(x=35, y=35, z=35)
    macrophage_list.append(MacrophageCellData.create_cell(point=point))
    fungus_list.append(
        FungusCellData.create_cell(point=point,
                                   status=FungusCellData.Status.RESTING))

    macrophage_list.internalize_conidia(1, 50, 1, grid, fungus_list)
    assert fungus_list.cell_data['internalized'][0]

    # simulate death
    macrophage_list.clear_all_phagosome(0, fungus_list)

    assert not fungus_list.cell_data['internalized'][0]
    assert macrophage_list.len_phagosome(0) == 0
コード例 #13
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def test_damage_conidia(macrophage_list: MacrophageCellList,
                        grid: RectangularGrid, fungus_list: FungusCellList):
    kill = 2
    t = 1
    health = 100

    point = Point(x=35, y=35, z=35)
    macrophage_list.append(MacrophageCellData.create_cell(point=point))
    fungus_list.append(
        FungusCellData.create_cell(point=point,
                                   status=FungusCellData.Status.RESTING))

    macrophage_list.internalize_conidia(1, 50, 1, grid, fungus_list)

    macrophage_list.damage_conidia(kill, t, health, fungus_list)

    assert fungus_list.cell_data['health'][0] == 50

    macrophage_list.damage_conidia(kill, t, health, fungus_list)

    assert fungus_list.cell_data['health'][0] == 0
コード例 #14
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def test_internalize_and_move(
    macrophage_list: MacrophageCellList,
    grid: RectangularGrid,
    fungus_list: FungusCellList,
    cyto,
    tissue,
):
    point = Point(x=35, y=35, z=35)
    macrophage_list.append(MacrophageCellData.create_cell(point=point))

    fungus_list.append(
        FungusCellData.create_cell(point=point,
                                   status=FungusCellData.Status.RESTING))
    fungus_list.append(
        FungusCellData.create_cell(point=point,
                                   status=FungusCellData.Status.RESTING))

    macrophage_list.internalize_conidia(1, 50, 1, grid, fungus_list)

    assert fungus_list.cell_data['internalized'][0]
    assert fungus_list.cell_data['internalized'][1]
    assert macrophage_list.len_phagosome(0) == 2

    rec_r = 10

    cell = macrophage_list[0]
    vox = grid.get_voxel(cell['point'])
    assert vox.z == 3 and vox.y == 3 and vox.x == 3

    assert cyto.all() == 0
    cyto[4, 3, 3] = 10

    macrophage_list.move(rec_r, grid, cyto, tissue, fungus_list)

    vox = grid.get_voxel(cell['point'])
    assert vox.z == 4 and vox.y == 3 and vox.x == 3

    for f in fungus_list:
        vox = grid.get_voxel(f['point'])
        assert vox.z == 4 and vox.y == 3 and vox.x == 3
コード例 #15
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def test_update(
    neutrophil_list: NeutrophilCellList, grid: RectangularGrid, fungus_list: FungusCellList, iron
):
    n_det = 1
    n_kill = 2
    t = 1
    health = 100

    point = Point(x=35, y=35, z=35)
    neutrophil_list.append(
        NeutrophilCellData.create_cell(
            point=point, status=NeutrophilCellData.Status.NONGRANULATING, granule_count=2
        )
    )

    fungus_list.append(
        FungusCellData.create_cell(
            point=point, status=FungusCellData.Status.RESTING, form=FungusCellData.Form.HYPHAE
        )
    )
    fungus_list.append(
        FungusCellData.create_cell(
            point=Point(x=45, y=35, z=35),
            status=FungusCellData.Status.RESTING,
            form=FungusCellData.Form.HYPHAE,
        )
    )

    neutrophil_list.damage_hyphae(n_det, n_kill, t, health, grid, fungus_list, iron)

    assert fungus_list[0]['health'] == 50
    assert fungus_list[1]['health'] == 50
    assert neutrophil_list[0]['granule_count'] == 0
    assert neutrophil_list[0]['status'] == NeutrophilCellData.Status.GRANULATING

    neutrophil_list.update()

    assert neutrophil_list[0]['status'] == NeutrophilCellData.Status.NONGRANULATING
コード例 #16
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def test_internalize_conidia_none(
    populated_macrophage: MacrophageCellList,
    grid: RectangularGrid,
    populated_fungus: FungusCellList,
):
    m_det = 0

    cell = populated_macrophage[0]
    vox = grid.get_voxel(cell['point'])
    assert len(populated_fungus.get_cells_in_voxel(vox)) == 1

    populated_macrophage.internalize_conidia(m_det, 50, 1, grid,
                                             populated_fungus)

    assert populated_macrophage.len_phagosome(0) == 0
    for v in cell['phagosome']:
        assert v == -1
コード例 #17
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def test_damage_hyphae_granuleless(
    neutrophil_list: NeutrophilCellList, grid: RectangularGrid, fungus_list: FungusCellList, iron
):
    n_det = 1
    n_kill = 2
    t = 1
    health = 100

    point = Point(x=35, y=35, z=35)
    neutrophil_list.append(
        NeutrophilCellData.create_cell(
            point=point, status=NeutrophilCellData.Status.NONGRANULATING, granule_count=2
        )
    )

    fungus_list.append(
        FungusCellData.create_cell(
            point=point, status=FungusCellData.Status.RESTING, form=FungusCellData.Form.HYPHAE
        )
    )
    fungus_list.append(
        FungusCellData.create_cell(
            point=Point(x=45, y=35, z=35),
            status=FungusCellData.Status.RESTING,
            form=FungusCellData.Form.HYPHAE,
        )
    )
    fungus_list.append(
        FungusCellData.create_cell(
            point=Point(x=25, y=35, z=35),
            status=FungusCellData.Status.RESTING,
            form=FungusCellData.Form.HYPHAE,
        )
    )

    neutrophil_list.damage_hyphae(n_det, n_kill, t, health, grid, fungus_list, iron)

    assert fungus_list[0]['health'] == 50
    # one should be 50, the other 100. It doesn't matter which is which
    assert fungus_list[1]['health'] == 100 or fungus_list[2]['health'] == 100
    assert fungus_list[1]['health'] == 50 or fungus_list[2]['health'] == 50
    assert neutrophil_list[0]['granule_count'] == 0
    assert neutrophil_list[0]['status'] == NeutrophilCellData.Status.NONGRANULATING
コード例 #18
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ファイル: test_fungus.py プロジェクト: knappa/nlisim
def fungus_list(grid: RectangularGrid):
    fungus = FungusCellList(grid=grid)
    yield fungus
コード例 #19
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def test_internalize_conidia_n(macrophage_list: MacrophageCellList,
                               grid: RectangularGrid,
                               fungus_list: FungusCellList):

    point = Point(x=35, y=35, z=35)
    macrophage_list.append(MacrophageCellData.create_cell(point=point))

    fungus_list.append(
        FungusCellData.create_cell(point=point,
                                   status=FungusCellData.Status.RESTING))
    fungus_list.append(
        FungusCellData.create_cell(point=point,
                                   status=FungusCellData.Status.RESTING))

    point = Point(x=45, y=35, z=35)
    fungus_list.append(
        FungusCellData.create_cell(point=point,
                                   status=FungusCellData.Status.RESTING))
    fungus_list.append(
        FungusCellData.create_cell(point=point,
                                   status=FungusCellData.Status.RESTING))

    point = Point(x=55, y=35, z=35)
    fungus_list.append(
        FungusCellData.create_cell(point=point,
                                   status=FungusCellData.Status.RESTING))
    fungus_list.append(
        FungusCellData.create_cell(point=point,
                                   status=FungusCellData.Status.RESTING))

    # internalize some not all
    macrophage_list.internalize_conidia(1, 50, 1, grid, fungus_list)

    assert fungus_list.cell_data['internalized'][0]
    assert fungus_list.cell_data['internalized'][2]
    assert macrophage_list.len_phagosome(0) == 4

    # internalize all
    macrophage_list.internalize_conidia(2, 50, 1, grid, fungus_list)

    assert fungus_list.cell_data['internalized'][5]
    assert macrophage_list.len_phagosome(0) == 6