CN108467849A - 一种皮肤细胞分散液 - Google Patents

一种皮肤细胞分散液 Download PDF

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CN108467849A
CN108467849A CN201810183102.XA CN201810183102A CN108467849A CN 108467849 A CN108467849 A CN 108467849A CN 201810183102 A CN201810183102 A CN 201810183102A CN 108467849 A CN108467849 A CN 108467849A
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cell
digestion
dispersion liquid
skin
60min
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高文超
高文涛
乐畅
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Guangdong Xiangsheng New Material Technology Co.,Ltd.
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Guangzhou Towards Biological Technology Co Ltd
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    • C12N5/00Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
    • C12N5/06Animal cells or tissues; Human cells or tissues
    • C12N5/0602Vertebrate cells
    • C12N5/0625Epidermal cells, skin cells; Cells of the oral mucosa
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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    • C12N2509/00Methods for the dissociation of cells, e.g. specific use of enzymes

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Abstract

本发明提供了一种适用于快速消化分解皮肤活组织的混合液,该悬液可以将皮肤组织分散为单个细胞,加入细胞基质后进行扩增培养。

Description

一种皮肤细胞分散液
技术领域
本发明涉及生物医药领域,特别涉及了一种适用于快速消化分解皮肤活组织的混合液,该悬液可以将皮肤组织分散为单个细胞,加入细胞基质后进行扩增培养。
背景技术
细胞培养是生物学和医学研究最常用的手段之一,可分为原代培养和传代培养两种。原代培养是直接从生物体获取细胞进行培养。进行原代培养可为研究生物体细胞的生长、代谢、繁殖提供有力的手段,同时也为以后传代培养创造条件,因为细胞刚刚从活体组织分离出来,更接近于生物体内的生活状态。利用此方法还可直接服务于临床实践。
进行原代培养的关键步骤在于将取代的样本消化为单个活细胞,这一限速步骤关系到原代培养的成功与否。现有的方法主要包括机械法或化学法,干扰因素较多,成功几率不高。
发明内容
在本发明提供了一种适用于快速消化分解皮肤活组织的混合液,该悬液可以将皮肤组织分散为单个细胞,加入细胞基质后进行扩增培养。
技术方案如下:
1. 实验准备:
实验解剖器材(眼科剪,眼科镊,手术刀,200目细胞筛)高压灭菌121℃ 20min
25ml Hu16培养基的配制:
20ng/ml bFGF +10ng/ml CT+ 20μg/ml IBMX
+1*gentamicin
+10%FBS
+1*青链霉素溶液
+DMEM/F12
2.取皮
皮肤样本处理:将皮肤组织用手术刀裁成1cm2大小,共5份,然后用0.01MPBS(含1%双抗)洗涤2-3次。
3.分散消化
用新的眼科剪和眼科镊将1cm2皮肤剪碎,约1mm3大小,移入含20ml 0.25%胰酶的50ml离心管中;
将5个离心管置于37℃水浴锅中,消化30-60min。
消化方案如表1
表1:
消化时,每5min颠倒混匀一次,使胰酶于皮肤组织充分接触,于30min和60min取细胞悬液做台盼蓝染色并计数活细胞数目。
台盼蓝染色步骤:
1.、4%台盼蓝母液:称取4g台盼蓝,加少量蒸馏水研磨,加双蒸水至100ml,用滤纸过滤,4度保存。使用时,用PBS稀释至0.4%。
3、染色:细胞悬液与0.4%台盼蓝溶液以9:1混合混匀。(终浓度0.04%)
4、计数:在5分钟内,分别计数活细胞和死细胞。
5、镜下观察,死细胞被染成明显的蓝色,而活细胞拒染呈无色透明状。
6、统计细胞活力:活细胞率(%)= 活细胞总数/(活细胞总数+死细胞总数)×100%
结果:镜下观察细胞,未见明显死细胞,大多数细胞保持完整细胞膜结构。细胞计数:胰酶0.25%-0.15%消化30min,细胞数105数量级;胰酶0.25%-0.15%消化60min,细胞数有所减少。
4.培养
消化60min后,200目细胞筛过滤,滤液转移至新的50ml离心管中,750rpm离心5min,1500rpm离心5min,弃上清
用0.01MPBS(含1%双抗)洗涤1次,1500rpm离心5min,弃上清
用完全培养基重悬细胞,接种于6孔板中,于37℃ 5%CO2 95%湿度培养箱中培养并观察。
胰酶浓度设置:0.25% 0.20% 0.15% 消化15min 20min 30min,其他同上
优选的,0.25% 0.20%胰酶消化皮肤组织,消化15-20min细胞计数达108数量级。最终确认0.25%胰酶消化15-20min为 最佳选择。
上述实施方式只为说明本发明的技术构思及特点,其目的在于让熟悉此项技术的人能够了解本发明的内容并据以实施,并不能以此限制本发明的保护范围。凡根据本发明精神实质所做的等效变换或修饰,都应涵盖在本发明的保护范围之内。

Claims (6)

1.一种皮肤分散液,其特征在于快速消化分解皮肤活组织。
2.如权利要求2所述的分散液,特征在于可以将皮肤组织分散为单个细胞,加入细胞基质后进行扩增培养。
3.如权利要求1所述的分散液消化的皮肤组织样本,特征在于来源人的上皮。
4.如权利要求3所述的方法取得的皮肤样本,进行消化分散的主要步骤如下:
1)将样本用剪刀剪碎约1mm3大小;
2)用0.01MPBS(含1%双抗)洗涤2-3次;
3)加分散液;
4)置于37℃水浴锅中,消化30-60min;
5)于30min和60min取细胞悬液,台盼蓝染色并计数活细胞数目;
6)消化60min后,200目细胞筛过滤;
7)用0.01MPBS(含1%双抗)洗涤1次,1500rpm离心5min,弃上清;
8)用完全培养基重悬细胞,接种于6孔板中,于37℃ 5%CO2 95%湿度培养箱中培养并观察。
5.如权利要求4中所述的步骤,特征在于皮肤样本要用眼科剪和眼科镊剪碎,优选的,约1mm3大小。
6.如权利要求4中所述的消化,特征在于消化时,每5min颠倒混匀一次,使于皮肤组织充分接触。
CN201810183102.XA 2018-03-06 2018-03-06 一种皮肤细胞分散液 Pending CN108467849A (zh)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114652662A (zh) * 2020-12-23 2022-06-24 天津拂瑞雅生物科技有限公司 修复霜及其制备方法

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104059874A (zh) * 2014-04-10 2014-09-24 金华市农业科学研究院 金华猪耳真皮成纤维细胞系的构建方法

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104059874A (zh) * 2014-04-10 2014-09-24 金华市农业科学研究院 金华猪耳真皮成纤维细胞系的构建方法

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
XUEHUI HE 等: "Lymphocyte Isolation from Human Skin for Phenotypic Analysis and Ex Vivo Cell Culture", 《JOURNAL OF VISUALIZED EXPERIMENTS : JOVE》 *
中国标准物质网: "单细胞的制备与培养", 《HTTP://WWW.GBW114.COM/NEWS/N23255.HTML》 *
伍津津: "《皮肤组织工程学》", 30 June 2009, 人民军医出版社 *
崔正军 等: "用于祛除皱纹的真皮成纤维细胞体外培养的研究", 《中华损伤与修复杂志》 *
窦肇华等: "《免疫细胞学与疾病》", 30 September 2004, 中国医药科技出版社 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114652662A (zh) * 2020-12-23 2022-06-24 天津拂瑞雅生物科技有限公司 修复霜及其制备方法

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